Aki S. Havulinna
Nature Genetics · 2008–2023
A researcher in the Science corpus: 20 papers; trusts 0 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Who trusts Aki S. Havulinna overall
Papers from Aki S. Havulinna's perspective
Ordered by how strongly the researchers Aki S. Havulinna trusts endorse each paper. Same corpus, a different order for every researcher.
- Next-generation genotype imputation service and methods (Nature Genetics)
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology (Statistics in Medicine)
- Clinical use of current polygenic risk scores may exacerbate health disparities
- Sex Hormone–Binding Globulin and Risk of Type 2 Diabetes in Women and Men (New England Journal of Medicine)
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (Nature Genetics)
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
- Fast and accurate long-range phasing in a UK Biobank cohort
Their papers
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (2015) — 774 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Greengenes2 unifies microbial data in a single reference tree (2023) — 563 citations
- FinnGen provides genetic insights from a well-phenotyped isolated population (2023) — 3,553 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease (2019) — 13 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Geographic variation and bias in polygenic scores of complex diseases and traits in Finland (2018) — 32 citations
- Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (2017) — 114 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Effects of long-term exposure to air pollution on natural-cause mortality: an analysis of 22 European cohorts within the multicentre ESCAPE project. (2014) — 1,229 citations
- Genetic Risk Prediction and a Two-Stage Risk Screening Strategy for Coronary Heart Disease (2013) — 162 citations
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) — 2,232 citations
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) — 3,781 citations
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) — 973 citations
- Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans (2008) — 1,459 citations
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2008) — 1,801 citations